Gunnar Sjöberg

Om mig
Publikationer
Forskningsbidrag
Populärvetenskap och samverkan

Om mig

Forskare och överläkare på Barnhjärtcentrum med speciell inriktning mot
interventionell barnkardiologi och kardiogenetik. FOU-ansvarig inom enheten
för barnkardiologi och ledamot av FOU grupp inom ME/OO HBM2.

Forskningsbeskrivning

Med min bakgrund inom molekylärbiologisk grundforskning på muskelceller var
det naturligt att som kliniker intressera mig för patientgruppen barn med
ärftliga hjärtmuskelsjukdomar (kardiomyopatier). Min forskning har därför
rört genetiska och molekylära aspekter på dessa sjukdomar och
laboratorieverksamheten har tidigare varit på CMM följt av Bioclinicum här
på KI med ett nära samarbete med Almazov Medical Center i St Petersburg.
Som interventionell barnkardiolog har forskning inom även detta fält på
senare år tagit plats med studier av öppetstående ductus arteriosus och
förmaksseptumdefekter framför allt hos för tidigt födda barn. Som
huvudhandledare för Eva Rylander Hedlund också slutfört ett
doktorandprojekt med studier av fysisk aktivitet hos barn med
enkammarhjärta.

Artiklar

Article: JACC-CARDIOVASCULAR INTERVENTIONS. 2023;16(4):444-453

Transcatheter Intervention for Coarctation of the Aorta: A Nordic Population-Based Registry With Long-Term Follow-Up.

Eriksson P; Pihkala J; Jensen AS; Dohlen G; Liuba P; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Leirgul E; Settergren M; Vithessonthi K; Nielsen N-E; Christersson C; Sondergaard L; Sinisalo J; Nielsen-Kudsk JE; Dellborg M; Larsen SH
Article: ORPHANET JOURNAL OF RARE DISEASES. 2022;17(1):358

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.

Muravyev A; Vershinina T; Tesner P; Sjoberg G; Fomicheva Y; Čajbiková NN; Kozyreva A; Zhuk S; Mamaeva E; Tarnovskaya S; Jornholt J; Sokolnikova P; Pervunina T; Vasichkina E; Sejersen T; Kostareva A
Article: CARDIOLOGY IN THE YOUNG. 2022;32(6):861-868

Vitamin D, liver-related biomarkers, and distribution of fat and lean mass in young patients with Fontan circulation.

Hansson L; Sandberg C; Öhlund I; Lind T; Sthen Bergdahl M; Wiklund U; Rylander Hedlund E; Sjöberg G; Rydberg A
Article: JOURNAL OF THE AMERICAN HEART ASSOCIATION. 2022;11(7):e022929

Impact of Left Ventricular Morphology on Adverse Outcomes Following Stage 1 Palliation for Hypoplastic Left Heart Syndrome: 20 Years of National Data From Sweden.

Fricke K; Mellander M; Hanséus K; Tran P-K; Synnergren M; Johansson Ramgren J; Rydberg A; Sunnegårdh J; Dalén M; Sjöberg G; Weismann CG; Liuba P
Article: PEDIATRIC CARDIOLOGY. 2022;43(2):449-456

Calf Muscle Oxygenation is Impaired and May Decline with Age in Young Patients with Total Cavopulmonary Connection.

Bergdahl MS; Crenshaw AG; Hedlund ER; Sjöberg G; Rydberg A; Sandberg C
Article: ACTA PAEDIATRICA. 2021;110(11):3105-3115

Sudden cardiac death in childhood hypertrophic cardiomyopathy is best predicted by a combination of electrocardiogram risk-score and HCMRisk-Kids score.

Östman-Smith I; Sjöberg G; Alenius Dahlqvist J; Larsson P; Fernlund E
Article: JOURNAL OF CLINICAL MEDICINE. 2020;10(1):E122-122

Right Heart Structure, Geometry and Function Assessed by Echocardiography in 6-Year-Old Children Born Extremely Preterm-A Population-Based Cohort Study.

Mohlkert L-A; Hallberg J; Broberg O; Sjöberg G; Rydberg A; Liuba P; Fellman V; Domellöf M; Norman M; Halvorsen CP
Journal article: EUROPEAN HEART JOURNAL. 2020;41(Supplement_2):ehaa946.2193-

Transcatheter interventions of coarctation of the aorta (CoA): a multinational population-based registry – procedural complications

Eriksson P; NoCoAS; Pikhala J; Jensen AS; Dohlen G; Liuba P; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Dellborg M; Settergren M; Kudsk JEN; Sondergaard L; Sinisalo J; Holm S
Journal article: CARDIOLOGY IN THE YOUNG. 2020;30(8):1138-1143

Impaired knee extension muscle strength in adolescents but not in children with Fontan circulation.

Sandberg C; Frisk E; Hansson L; Isberg A; Rylander Hedlund E; Sjöberg G; Rydberg A
Article: ACTA PAEDIATRICA. 2020;109(4):746-753

Lung function and pulmonary vascular resistance are not associated in 6-year-old children born extremely preterm.

Mohlkert L-A; Sjöberg G; Rydberg A; Pegelow Halvorsen C; Tufvesson E; Hallberg J; Domellöf M; Norman M
Article: JOURNAL OF CARDIAC SURGERY. 2020;35(4):868-874

Long-term results of aortic arch reconstruction with branch pulmonary artery homograft patches.

Lewis MJ; Johansson Ramgren J; Hallbergson A; Liuba P; Sjöberg G; Malm T
Article: CARDIOLOGY IN THE YOUNG. 2020;30(3):303-312

Risk factors for adverse events within one year after atrial septal closure in children: a retrospective follow-up study.

Tanghöj G; Liuba P; Sjöberg G; Naumburg E
Article: PLOS ONE. 2020;15(3):e0229227

Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments.

Cimiotti D; Fujita-Becker S; Möhner D; Smolina N; Budde H; Wies A; Morgenstern L; Gudkova A; Sejersen T; Sjöberg G; Mügge A; Nowaczyk MM; Reusch P; Pfitzer G; Stehle R; Schröder RR; Mannherz HG; Kostareva A; Jaquet K
Article: CARDIOLOGY. 2020;145(11):746-756

Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients.

Vershinina T; Fomicheva Y; Muravyev A; Jorholt J; Kozyreva A; Kiselev A; Gordeev M; Vasichkina E; Segrushichev A; Pervunina T; Sjoberg G; Skyttner-Rahmani S; Sejersen T; Kostareva A
Article: CONGENITAL HEART DISEASE. 2020;15(5):287-299

Atrial Septal Defect in Children: The Incidence and Risk Factors for Diagnosis

Tanghoj G; Lindam A; Liuba P; Sjoberg G; Naumburg E
Article: CARDIOLOGY IN THE YOUNG. 2019;29(7):922-929

Physical exercise may improve sleep quality in children and adolescents with Fontan circulation.

Hedlund ER; Villard L; Lundell B; Sjöberg G
Article: CARDIOLOGY IN THE YOUNG. 2019;29(5):626-636

Adverse events within 1 year after surgical and percutaneous closure of atrial septal defects in preterm children.

Tanghöj G; Liuba P; Sjöberg G; Rydberg A; Naumburg E
Article: FRONTIERS IN GENETICS. 2019;10:608

Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy.

Kiselev A; Vaz R; Knyazeva A; Sergushichev A; Dmitrieva R; Khudiakov A; Jorholt J; Smolina N; Sukhareva K; Fomicheva Y; Mikhaylov E; Mitrofanova L; Predeus A; Sjoberg G; Rudenko D; Sejersen T; Lindstrand A; Kostareva A
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2019;6:185

Predictors of the Need for an Atrial Septal Defect Closure at Very Young Age.

Tanghöj G; Liuba P; Sjöberg G; Naumburg E
Article: CARDIOLOGY IN THE YOUNG. 2018;28(9):1115-1122

Impaired lung function in children and adolescents with Fontan circulation may improve after endurance training.

Hedlund ER; Ljungberg H; Söderström L; Lundell B; Sjöberg G
Article: HUMAN MUTATION. 2018;39(9):1161-1172

De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.

Kiselev A; Vaz R; Knyazeva A; Khudiakov A; Tarnovskaya S; Liu J; Sergushichev A; Kazakov S; Frishman D; Smolina N; Pervunina T; Jorholt J; Sjoberg G; Vershinina T; Rudenko D; Arner A; Sejersen T; Lindstrand A; Kostareva A
Article: CARDIOLOGY IN THE YOUNG. 2018;28(3):438-446

Can endurance training improve physical capacity and quality of life in young Fontan patients?

Hedlund ER; Lundell B; Söderström L; Sjöberg G
Article: JOURNAL OF THE AMERICAN HEART ASSOCIATION. 2018;7(2):e007742

The Preterm Heart in Childhood: Left Ventricular Structure, Geometry, and Function Assessed by Echocardiography in 6-Year-Old Survivors of Periviable Births.

Mohlkert L-A; Hallberg J; Broberg O; Rydberg A; Halvorsen CP; Liuba P; Fellman V; Domellöf M; Sjöberg G; Norman M
Article: FRONTIERS IN GENETICS. 2018;9:684

Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy.

Knyazeva A; Krutikov A; Golovkin A; Mishanin A; Pavlov G; Smolina N; Hushkina A; Sejersen T; Sjoberg G; Galagudza M; Kostareva A
Journal article: EUROPEAN HEART JOURNAL. 2017;38(suppl_1)

P1606Mutation in MYOF gene is associated with ventricular arrhythmias and limb girdle muscle phenotype

Kiselev A; Dmitrieva R; Smolina N; Khudiakov A; Sergushichev A; Mikhailov E; Mitrophanova L; Rudenko D; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Journal article: EUROPEAN HEART JOURNAL. 2017;38(suppl_1)

P5404Hotspot mutation in FLNC gene as a cause of restrictive cardiomyopathy associated with congenital myopathy development

Kiselev A; Knyazeva A; Sergushichev A; Hudiakov A; Pervunina T; Vershinina T; Nikitina I; Rudenko D; Vasichkina E; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Article: PEDIATRIC RESEARCH. 2017;81(2):299-306

Preterm arteries in childhood: dimensions, intima-media thickness, and elasticity of the aorta, coronaries, and carotids in 6-y-old children born extremely preterm.

Mohlkert L-A; Hallberg J; Broberg O; Hellström M; Pegelow Halvorsen C; Sjöberg G; Edstedt Bonamy A-K; Liuba P; Fellman V; Domellöf M; Norman M
Article: OPEN HEART. 2017;4(2):e000658

Predictors of risk for sudden death in childhood hypertrophic cardiomyopathy: the importance of the ECG risk score.

Östman-Smith I; Sjöberg G; Rydberg A; Larsson P; Fernlund E
Article: ACTA PAEDIATRICA. 2016;105(11):1322-1328

Reduced physical exercise and health-related quality of life after Fontan palliation.

Hedlund ER; Lundell B; Villard L; Sjöberg G
Article: PLOS ONE. 2016;11(9):e0163362

Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing.

Kostareva A; Kiselev A; Gudkova A; Frishman G; Ruepp A; Frishman D; Smolina N; Tarnovskaya S; Nilsson D; Zlotina A; Khodyuchenko T; Vershinina T; Pervunina T; Klyushina A; Kozlenok A; Sjoberg G; Golovljova I; Sejersen T; Shlyakhto E
Journal article: KARDIOLOGIIA. 2016;17(4):278-286

Genetic variants of cardiomyopathies with the neuromuscular phenotype

Kostareva AA; Pervunina TM; Moiseeva OM; Vershinina TL; Gudkova AY; Romanova EI; Kozlova SN; Rudenko DI; Sejersen T; Sjoberg G; Shlyakhto EV
Article: MOLECULAR GENETICS AND METABOLISM. 2015;115(2-3):118-127

Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner.

Malashicheva A; Bogdanova M; Zabirnyk A; Smolina N; Ignatieva E; Freilikhman O; Fedorov A; Dmitrieva R; Sjöberg G; Sejersen T; Kostareva A
Article: BIOMED RESEARCH INTERNATIONAL. 2015;2015:594751-12

Primary Murine Myotubes as a Model for Investigating Muscular Dystrophy.

Smolina N; Kostareva A; Bruton J; Karpushev A; Sjoberg G; Sejersen T
Journal article: ARCHIVES OF DISEASE IN CHILDHOOD. 2014;99(Suppl 2):a116

PS-012 Left Heart Structure And Function In 6-year-old Children Born Extremely Preterm

Mohlkert L; Broberg O; Hellström M; Halvorsen CP; Hallberg J; Sjöberg G; Bonamy AE; Fellman V; Domellöf M; Norman M
Article: CELL CALCIUM. 2014;56(4):269-275

Aggregate-prone desmin mutations impair mitochondrial calcium uptake in primary myotubes.

Smolina N; Bruton J; Sjoberg G; Kostareva A; Sejersen T
Article: CONGENITAL HEART DISEASE. 2014;9(5):391-396

Variants in the NOTCH1 gene in patients with aortic coarctation.

Freylikhman O; Tatarinova T; Smolina N; Zhuk S; Klyushina A; Kiselev A; Moiseeva O; Sjoberg G; Malashicheva A; Kostareva A
Article: PEDIATRIC CARDIOLOGY. 2013;34(2):467-470

Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes.

Gudkova A; Kostareva A; Sjoberg G; Smolina N; Turalchuk M; Kuznetsova I; Rybakova M; Edstrom L; Shlyakhto E; Sejersen T
Journal article: ARCHIVES OF DISEASE IN CHILDHOOD. 2012;97(Suppl 2):a326-A327

1139 Right Heart Dimensions and Function at 6 Years-Of-Age Using 2D- and 3D-Echocardiography

Mohlkert L; Halvorsen C; Sjöberg G; Hallberg J; Norman M
Article: ACTA MYOLOGICA. 2011;30(1):42-45

Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.

Kostareva A; Sjoberg G; Gudkova A; Smolina N; Semernin E; Shlyakhto E; Sejersen T
Article: PEDIATRIC BLOOD & CANCER. 2010;54(4):579-584

Exercise echocardiography in asymptomatic survivors of childhood cancer treated with anthracyclines: a prospective follow-up study.

Sieswerda E; Kremer LCM; Vidmar S; De Bruin ML; Smibert E; Sjöberg G; Cheung MMH; Weintraub RG
Article: JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY. 2008;29(1):25-36

Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria.

Kostareva A; Sjöberg G; Bruton J; Zhang S-J; Balogh J; Gudkova A; Hedberg B; Edström L; Westerblad H; Sejersen T
Article: JOURNAL OF HEART AND LUNG TRANSPLANTATION. 2007;26(3):293-295

X-linked cardiomyopathy presenting as contracted endocardial fibroelastosis.

Sjoberg G; Chow CW; Cooper S; Weintraub RG
Article: ACTA MYOLOGICA. 2006;25(3):109-115

Desmin mutations in a St. Petersburg cohort of cardiomyopathies.

Kostareva A; Gudkova A; Sjoberg G; Kiselev I; Moiseeva O; Karelkina E; Goldfarb L; Schlyakhto E; Sejersen T
Article: HUMAN MUTATION. 2006;27(9):906-913

Variable pathogenic potentials of mutations located in the desmin alpha-helical domain.

Goudeau B; Rodrigues-Lima F; Fischer D; Casteras-Simon M; Sambuughin N; de Visser M; Laforet P; Ferrer X; Chapon F; Sjöberg G; Kostareva A; Sejersen T; Dalakas MC; Goldfarb LG; Vicart P
Article: EXPERIMENTAL CELL RESEARCH. 2006;312(9):1554-1565

Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation.

Bär H; Kostareva A; Sjöberg G; Sejersen T; Katus HA; Herrmann H
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2005;102(42):15099-15104

Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages.

Bär H; Mücke N; Kostareva A; Sjöberg G; Aebi U; Herrmann H
Journal article: EUROPEAN JOURNAL OF HEART FAILURE, SUPPLEMENT. 2005;4(1):25

107 Desmin mutations in patients with cardiomyopathies

Kostareva A; Sjoberg G; Gudkova A; Kiselev I; Schlyakhto E; Sejersen T
Journal article: EUROPEAN JOURNAL OF HEART FAILURE, SUPPLEMENT. 2003;2(1):15-16

113 Morphological features of cardiomyopathy in L345P desmin transgenic mice

Kostareva A; Sjoberg G; Amineva KH; Gudkova A; Sejersen T; Shlyakhto E
Article: ACTA NEUROPATHOLOGICA. 2002;104(5):493-504

Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutation.

Carlsson L; Fischer C; Sjöberg G; Robson RM; Sejersen T; Thornell L-E
Article: HUMAN MOLECULAR GENETICS. 1999;8(12):2191-2198

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation.

Sjöberg G; Saavedra-Matiz CA; Rosen DR; Wijsman EM; Borg K; Horowitz SH; Sejersen T
Article: PEDIATRIC RESEARCH. 1998;43(3):386-392

Pediatric rhabdomyosarcomas express the intermediate filament nestin.

Kobayashi M; Sjöberg G; Söderhäll S; Lendahl U; Sandstedt B; Sejersen T
Article: DIFFERENTIATION. 1997;61(3):151-159

Distribution of nestin in the developing mouse limb bud in vivo and in micro-mass cultures of cells isolated from limb buds.

Wroblewski J; Engström M; Edwall-Arvidsson C; Sjöberg G; Sejersen T; Lendahl U
Article: NEUROMUSCULAR DISORDERS. 1997;7(1):39-54

Tenascin-C expression correlates with macrophage invasion in Duchenne muscular dystrophy and in myositis.

Gullberg D; Velling T; Sjöberg G; Salmivirta K; Gaggero B; Tiger CF; Edström L; Sejersen T
Article: EXPERIMENTAL CELL RESEARCH. 1995;220(1):112-123

Analysis of fibronectin and vitronectin receptors on human fetal skeletal muscle cells upon differentiation.

Gullberg D; Sjöberg G; Velling T; Sejersen T
Article: DEVELOPMENTAL DYNAMICS. 1995;204(1):57-65

Up-regulation of a novel integrin alpha-chain (alpha mt) on human fetal myotubes.

Gullberg D; Velling T; Sjöberg G; Sejersen T
Journal article: EXPERIMENTAL CELL RESEARCH. 1994;214(2):447-458

Colocalization of nestin and vimentin/desmin in skeletal muscle cells demonstrated by three-dimensional fluorescence digital imaging microscopy.

Sjöberg G; Jiang WQ; Ringertz NR; Lendahl U; Sejersen T
Journal article: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 1994;53(4):416-423

Myofibers from Duchenne/Becker muscular dystrophy and myositis express the intermediate filament nestin.

Sjöberg G; Edström L; Lendahl U; Sejersen T
Visa fler

Alla övriga publikationer

Conference publication: PEDIATRIC CARDIOLOGY. 2022;43(8):1938-1939

Same Day Discharge of Patients After Persistent Foramen Ovale (PFO) Closure with GORE®CARDIOFORM Septal Occluder (GSO)

Steiner K; Sjoberg G; Damlin A; Settergren M
Conference publication: EUROPEAN HEART JOURNAL. 2020;41:2193

Transcatheter interventions of coarctation of the aorta (CoA): a multinational population-based registry - procedural complications

Eriksson P; Pikhala J; Jensen AS; Dohlen G; Liuba P; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Dellborg M; Settergren M; Kudsk JEN; Sondergaard L; Sinisalo J; Holm S
Conference publication: EUROPEAN HEART JOURNAL. 2020;41:2197

Transcatheter intervention of coarctation of the aorta (CoA): a multinational population-based registry - effect on hypertension

Eriksson P; Pihkala J; Jensen AS; Dohlen G; Liuba R; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Dellborg M; Settergren M; Kudsk-Nielsen JE; Sondergaard L; Sinisalo J; Larsen SH
Meeting abstract: CARDIOVASCULAR RESEARCH. 2018;114:S19

New variant in CMYA5 gene is associated with early-onset restrictive cardiomyopathy and autism-spectrum disorder

Kiselev A; Kornishina T; Sergushichev A; Smolina N; Klyushina A; Pervunina T; Bang ML; Sjoberg G; Sejersen T; Kostareva A
Meeting abstract: CARDIOVASCULAR RESEARCH. 2018;114:S22

Desmin mutations impair mitochondrial function by promoting mtDNA release

Smolina N; Khudiakov A; Sjoberg G; Sejersen T; Kostareva A
Conference publication: EUROPEAN HEART JOURNAL. 2017;38:344

Mutation in MYOF gene is associated with ventricular arrhythmias and limb girdle muscle phenotype

Kiselev A; Dmitrieva R; Smolina N; Khudiakov A; Sergushichev A; Mikhailov E; Mitrophanova L; Rudenko D; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Conference publication: EUROPEAN HEART JOURNAL. 2017;38:1145

Hotspot mutation in FLNC gene as a cause of restrictive cardiomyopathy associated with congenital myopathy development

Kiselev A; Knyazeva A; Sergushichev A; Hudiakov A; Pervunina T; Vershinina T; Nikitina I; Rudenko D; Vasichkina E; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2016;216:188-189

Progressive cardiac conduction disease associated with a DSP gene mutation.

Kiselev A; Mikhaylov E; Parmon E; Sjoberg G; Sejersen T; Tarnovskaya S; Nugnyi P; Mitrofanova L; Lebedev D; Kostareva A
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2015;184:272-273

Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes.

Pervunina T; Vershinina T; Kiselev A; Nikitina I; Grekhov E; Mitrofanova L; Sjoberg G; Kostareva A
Meeting abstract: CARDIOVASCULAR RESEARCH. 2014;103:s104-s105

Genetic spectrum of idiopathic restrictive cardiomyopathy uncovered by new generation sequencing

Kostareva A; Gudkova A; Kiselev A; Zlotina A; Smolina N; Klyushina A; Hodyuchenko T; Sjoberg G; Sejersen T; Shlyakhto E
Meeting abstract: CARDIOVASCULAR RESEARCH. 2014;103:s73

Aggregate prone desmin mutations reduced mitochondrial calcium uptake in primary myotubes upon electrical stimulation

Smolina N; Bruton J; Sjoberg G; Kostareva A; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2014;35:534

Genetic spectrum of idiopathic restrictive cardiomyopathy uncovered by NGS

Kostareva A; Gudkova A; Kiselev A; Zlotina A; Klyushina A; Hodyuchenko T; Smolina N; Sjoberg G; Sejersen T; Shlyakhto E
Conference publication: EUROPEAN HEART JOURNAL. 2014;35:109

Aggregate prone desmin mutations reduced mitochondrial calcium uptake in primary myotubes upon electrical stimulation

Kostareva A; Smolina N; Bruton J; Sjoberg G; Sejersen T
Review: FRONTIERS IN BIOSCIENCE - SCHOLAR. 2013;5(1):325-340

Genetic spectrum of cardiomyopathies with neuromuscular phenotype.

Kostareva A; Sejersen T; Sjoberg G
Conference publication: CARDIOVASCULAR RESEARCH. 2010;87:S72

A213V desmin substitution represents a rare polymorphism rather than disease-causing mutation and is more prevalent in patients with heart dilation of various origins.

Kostareva A; Malashicheva A; Sjoberg G; Gudkova A; Semernin E; Shlyakhto E; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2010;31:924-925

Desmin L345P transgenic mice exhibit morphological and biochemical features of amyloidosis of two distinct types

Klingstedt T; Kostareva A; Sjoberg G; Gudkova A; Nilsson P; Hammarstrom P; Sejersen T
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2009;131(3):410-412

Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.

Kostareva A; Gudkova A; Sjöberg G; Mörner S; Semernin E; Krutikov A; Shlyakhto E; Sejersen T
Published conference paper: CELL BIOLOGY AND TRANSLATIONAL MEDICINE, VOL 14: STEM CELLS IN LINEAGE SPECIFIC DIFFERENTIATION AND DISEASE. 2009;652:13-21

Standards of care for Duchenne muscular dystrophy: brief TREAT-NMD recommendations.

Sejerson T; Bushby K; TREAT-NMD EU Network of Excellence
Conference publication: EUROPEAN JOURNAL OF CELL BIOLOGY. 2008;87(7):449-450

L345P desmin transgenic mice exhibit changes in mitochondrial Ca²⁺ handling

Kostareva A; Bruton J; Sjoberg G; Gudkova A; Westerblad H; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2007;28:795

L345P desmin transgenic mice exhibit changes in mitochondrial Ca²⁺ handling

Kostareva A; Bruton J; Sjoberg G; Gudkova A; Westerblad H; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2006;27:542

Deletion in the cardiac troponin I gene, resulting in premature stop codon, causes restrictive cardiomyopathy

Kostareva A; Gudkova A; Sjoberg G; Morner S; Semernin E; Krutikov A; Schlyakhto E; Sejersen TH
Review: LAKARTIDNINGEN. 2005;102(11):845-853

[Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].

Sjöberg G; Kostareva A; Sejersen T
Conference publication: EUROPEAN JOURNAL OF CELL BIOLOGY. 2005;84:97

Missense mutations of desmin corrupt filament formation at various stages of the assembly process

Bär H; Mücke N; Kostareva A; Sjöberg G; Aebi U; Herrmann H
Review: JOURNAL OF STRUCTURAL BIOLOGY. 2004;148(2):137-152

The biology of desmin filaments: how do mutations affect their structure, assembly, and organisation?

Bär H; Strelkov SV; Sjöberg G; Aebi U; Herrmann H
Conference publication: NEUROMUSCULAR DISORDERS. 2004;14(8-9):594

Morphological features of cardiomyopathy in L345P desmin transgenic mice

Kostareva A; Sjöberg G; Gudkova A; Zhang S; Westerblad H; Sejersen T
Conference publication: EUROPEAN JOURNAL OF CELL BIOLOGY. 2004;83:39

Molecular analysis of mutations causing human desmin-related myopathy (DRM)

Bär H; Sjöberg G; Herrmann H
Meeting abstract: EUROPEAN HEART JOURNAL. 2003;24:695

Morphological features of cardiomyopathy in L345P desmin mutation

Kostareva A; Sjoberg G; Gudkova A; Rybakova M; Sejersen T; Shlyakhto E
Conference publication: NEUROMUSCULAR DISORDERS. 2003;13(7-8):629

Functional analyses of L345P desmin mutation associated with familial myopathy and cardiomyopathy

Kostareva A; Sjöberg G; Gudkova A; Sejersen T
Conference publication: MOLECULAR BIOLOGY OF THE CELL. 1997;8:2272

Nestin forms obligate heteropolymers with desmin and vimentin in vivo.

Sjoberg G; Meng JJ; Sejersen T; Ip W
Published conference paper: ANNALS OF THE NEW YORK ACADEMY OF SCIENCES. 1996;785:353-355

Nestin distribution in the developing limb bud in vivo and in vitro.

Wroblewski J; Engström M; Edwall-Arvidsson C; Sjöberg G; Sejersen T; Lendahl U
Conference publication: JOURNAL OF CELLULAR BIOCHEMISTRY. 1994;:511

INTERMEDIATE FILAMENT NESTIN EXPRESSION DURING MYOGENESIS AND IN MUSCLE DISORDERS

SEJERSEN T; LENDAHL U; SJOBERG G; EDSTROM L
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